Associations between early tumor shrinkage/depth of response and survival from the ARCAD database.

IF 4.1 Q2 ONCOLOGY
Hideaki Bando, Yuriko Takeda, Toshihiro Misumi, Tomomi Nishikawa, Masashi Wakabayashi, Kentaro Yamazaki, Eiji Oki, Jean-Yves Douillard, Cornelis J A Punt, Miriam Koopman, Eric Van Cutsem, Carsten Bokemeyer, Alan P Venook, Heinz-Josef Lenz, Yoshihiko Maehara, Thierry Andre, Qian Shi, Aimery de Gramont, Takayuki Yoshino
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引用次数: 0

Abstract

Background: Early tumor shrinkage and depth of response have emerged as potential prognostic indicators in metastatic colorectal cancer (CRC). However, their associations with overall survival, progression-free survival (PFS), and postprogression survival in patients receiving anti-epidermal growth factor receptor (EGFR) antibodies or bevacizumab remain unclear.

Methods: We analyzed 3219 treatment-naive patients with RAS wild-type metastatic CRC from 8 randomized studies (CRYSTAL, OPUS, PRIME, CAIRO2, CALGB80405, WJOG4407G, ATOM, PARADIGM) in the Aid and Research in Digestive Cancerology database. Early tumor shrinkage was defined as a 20% or more reduction in tumor size at 8 ± 2 weeks, whereas depth of response was assessed by maximum tumor shrinkage at nadir. Cox regression models evaluated the associations of early tumor shrinkage and depth of response with overall survival, PFS, and postprogression survival, adjusting for confounders. A 2-sided test was conducted with a significance level of .05.

Results: Early tumor shrinkage and depth of response substantially stratified overall survival, PFS, and postprogression survival outcomes across all treatment groups. Early tumor shrinkage positivity was associated with improved overall survival, PFS, and postprogression survival in anti-EGFR and bevacizumab-based therapies, with a trend toward better outcomes in the anti-EGFR group. The depth of response analysis revealed optimal cutoff values of 0.55 for anti-EGFR-based therapy and 0.47 for bevacizumab-based therapy to achieve a median overall survival of approximately 32 months.

Conclusions: Early tumor shrinkage and depth of response serve as valuable prognostic markers in RAS wild-type metastatic CRC, particularly for patients treated with anti-EGFR antibodies. These findings highlight the potential role of early tumor shrinkage and depth of response in guiding treatment strategies and improving outcomes for patients with CRC.

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Abstract Image

Abstract Image

早期肿瘤缩小/反应深度与ARCAD数据库中存活之间的关系。
背景:早期肿瘤缩小(ETS)和反应深度(DpR)已成为转移性结直肠癌(mCRC)的潜在预后指标。然而,在接受抗表皮生长因子受体(anti- egfr)抗体或贝伐单抗治疗的患者中,它们与总生存期(OS)、无进展生存期(PFS)和进展后生存期(PPS)的关系尚不清楚。方法:我们分析了来自8个随机研究(CRYSTAL, OPUS, PRIME, CAIRO2, CALGB80405, WJOG4407G, ATOM, PARADIGM)的消化系统癌症分析与研究(ARCAD)数据库中的3,219例RAS野生型mCRC treatment-naïve患者。ETS被定义为在8±2周时肿瘤大小减少≥20%,而DpR是通过最低点时最大肿瘤缩小来评估的。Cox回归模型评估了ETS和DpR与OS、PFS和PPS的关系,并对混杂因素进行了调整。双侧检验,显著性水平为0.05。结果:ETS和DpR对所有治疗组的OS、PFS和PPS结果进行了显著分层。ETS阳性与抗egfr和贝伐单抗治疗中OS、PFS和PPS的改善相关,抗egfr组有更好的预后趋势。DpR分析显示,以抗egfr为基础的治疗的最佳截止值为0.55,以贝伐单抗为基础的治疗的最佳截止值为0.47,以实现约32个月的中位OS。结论:ETS和DpR在RAS野生型mCRC中是有价值的预后标志物,特别是对于接受抗egfr抗体治疗的患者。这些发现强调了ETS和DpR在指导治疗策略和改善患者预后方面的潜在作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
JNCI Cancer Spectrum
JNCI Cancer Spectrum Medicine-Oncology
CiteScore
7.70
自引率
0.00%
发文量
80
审稿时长
18 weeks
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